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Harrison I, Takeuchi Y, Bartosch B, et al. Determinants of high titer in recombinant porcine endogenous retroviruses. J Virol 2004; 78:13871-13879. The precise delineation of the determinants of high titer growth in human cells has confirmed PERV-C as a critical factor. By selecting animals lacking PERV-C expression, one will minimize the potential of generating the recombinant PERV, which is probably the greatest microbiological safety concern for xenotransplantation.
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Bartosch B, Stefandis D, Myers R, et al. Evidence and consequence of porcine endogenous retrovirus recombination. J Virol 2004; 78:13880-13890. This is a similar manuscript to Harrison et al., which also concludes safety advantages of using PERV-C negative donor pigs.
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Lavillette D, Kabat D. Porcine endogenous retroviruses infect cells lacking cognate receptors by an alternative pathway: implications for retrovirus evolution and xenotransplantation. J Virol 2004; 78:8868-8877.
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Ramachandran S, Jaramillo A, Xu XC, et al. Human immune responses to porcine endogenous retrovirus-derived peptides presented naturally in the context of porcine and human major histocompatibility complex class I molecules: implications in xenotransplantation of porcine organs. Transplantation 2004; 77:1580-1588.
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Binette TM, Seeberger KL, Lyon JG, et al. Porcine endogenous retroviral nucleic acid in peripheral tissues is associated with migration of porcine cells post islet transplant. Am J Transplant 2004; 4:1051-1060.
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Goto M, Maeda A, Elfman L, et al. No transmission of porcine endogenous retrovirus after transplantation of adult porcine islets into diabetic nude mice and immunosuppressed rats. Xenotransplantation 2004; 11:340-346.
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Kuddus RH, Metes DM, Nalesnik MA, et al. Porcine cell microchimerism but lack of productive porcine endogenous retrovirus (PERV) infection in naive and humanized SCID-beige mice treated with porcine peripheral blood mononuclear cells. Transpl Immunol 2004; 13:15-24.
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Irgang M, Karlas A, Laue C, et al. Porcine endogenous retroviruses PERV-A and PERV-B infect neither mouse cells in vitro nor SCID mice in vivo. Intervirology 2005; 48:167-173.
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Moscoso I, Hermida-Prieto M, Manez R, et al. Lack of cross-species transmission of porcine endogenous retrovirus in pig-to-baboon xenotransplantation with sustained depletion of anti-alphagal antibodies. Transplantation 2005; 79:777-782.
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Yang YG, Wood JC, Lan P, et al. Mouse retrovirus mediates porcine endogenous retrovirus transmission into human cells in long-term human-porcine chimeric mice. J Clin Invest 2004; 114:695-700. This study highlights the limitations to certain mouse models of PERV infection. More stringent models of PERV infectivity in vivo are required to generate a representative analysis of the factors that might influence PERV transmission in the clinic.
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Martina Y, Kurian S, Cherqui S, et al. Pseudotyping of porcine endogenous retrovirus by xenotropic murine leukemia virus in a pig islet xenotransplantation model. Am J Transplant 2005; 5:1837-1847. The further delineation of the role of murine viruses in PERV infectivity in vivo will allow for the improvement of safety studies in murine models.
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Am J Transplant
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